Canonical Allele Identifier: CA345439494

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241672077A>T (hg19) ; chr1:g.241508777A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508777A>T , CM000663.2:g.241508777A>T	GRCh38
NC_000001.10:g.241672077A>T , CM000663.1:g.241672077A>T	GRCh37
NC_000001.9:g.239738700A>T	NCBI36
NG_012338.1:g.15978T>A , LRG_504:g.15978T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1067T>A
ENST00000682162.1:c.593T>A	ENSP00000508203.1:n.593T>A
ENST00000682567.1:n.641T>A
ENST00000683521.1:c.564T>A	ENSP00000506864.1:p.Asn188Lys
ENST00000684161.1:n.1779T>A
ENST00000684483.1:c.556-17T>A	ENSP00000507894.1:n.556-17T>A
ENST00000366560.4:c.564T>A MANE Select	ENSP00000355518.4:p.Asn188Lys
ENST00000366560.3:c.564T>A	ENSP00000355518.3:p.Asn188Lys
NM_000143.3:c.564T>A , LRG_504t1:c.564T>A	NP_000134.2:p.Asn188Lys
XM_011544132.1:c.336T>A	XP_011542434.1:p.Asn112Lys
XM_011544132.2:c.336T>A	XP_011542434.1:p.Asn112Lys
NM_000143.4:c.564T>A MANE Select	NP_000134.2:p.Asn188Lys